<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Diaz-Ruiz R</submitter><funding>Brain &amp; Behavior Research Foundation</funding><funding>Instituto de Salud Carlos III</funding><funding>Ministerio de Ciencia, Innovación y Universidades</funding><funding>Fundacion Familia Alonso</funding><funding>Comunidad de Madrid</funding><pagination>226</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11768058</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(2)</volume><pubmed_abstract>&lt;b>Background/Objectives:&lt;/b> Decompensated cirrhosis is characterized by systemic inflammation and innate and adaptive immune dysfunction. Hepatic encephalopathy (HE) is a prevalent and debilitating condition characterized by cognitive disturbances in which ammonia and inflammation play a synergistic pathogenic role. Extraskeletal functions of vitamin D include immunomodulation, and its deficiency has been implicated in immune dysfunction and different forms of cognitive impairment. The aim was to assess changes in cognitive function and inflammation in decompensated patients with cirrhosis receiving vitamin D supplementation. &lt;b>Methods&lt;/b>: Patients with cirrhosis discharged from decompensation in two tertiary hospitals in Spain (from September 2017 to January 2020) were assessed before</pubmed_abstract><journal>Nutrients</journal><pubmed_title>Vitamin D Supplementation Is Associated with Inflammation Amelioration and Cognitive Improvement in Decompensated Patients with Cirrhosis.</pubmed_title><pmcid>PMC11768058</pmcid><funding_grant_id>RYC-2017-23144</funding_grant_id><funding_grant_id>NARSAD 24628</funding_grant_id><funding_grant_id>ICI20/00063 y PI21/00189</funding_grant_id><funding_grant_id>PI21/00701M PI24/01298</funding_grant_id><funding_grant_id>JR14/00019</funding_grant_id><funding_grant_id>S2022/BMD-7216 AGES 3-CM</funding_grant_id><funding_grant_id>PI16/00920</funding_grant_id><funding_grant_id>FI19/00120</funding_grant_id><funding_grant_id>CNS2023-144038</funding_grant_id><funding_grant_id>FFA-2024</funding_grant_id><pubmed_authors>Banares R</pubmed_authors><pubmed_authors>Lopez-Esteban R</pubmed_authors><pubmed_authors>Rapado-Castro M</pubmed_authors><pubmed_authors>Breton I</pubmed_authors><pubmed_authors>Poca M</pubmed_authors><pubmed_authors>Cuyas B</pubmed_authors><pubmed_authors>Soriano G</pubmed_authors><pubmed_authors>Garcia-Martinez R</pubmed_authors><pubmed_authors>Blazquez E</pubmed_authors><pubmed_authors>Morales A</pubmed_authors><pubmed_authors>Diaz-Ruiz R</pubmed_authors><pubmed_authors>Panadero-Gomez R</pubmed_authors><pubmed_authors>Fernandez-Castillo M</pubmed_authors><pubmed_authors>Roman E</pubmed_authors><pubmed_authors>Correa-Rocha R</pubmed_authors><pubmed_authors>Banares I</pubmed_authors><pubmed_authors>Puerto M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vitamin D Supplementation Is Associated with Inflammation Amelioration and Cognitive Improvement in Decompensated Patients with Cirrhosis.</name><description>&lt;b>Background/Objectives:&lt;/b> Decompensated cirrhosis is characterized by systemic inflammation and innate and adaptive immune dysfunction. Hepatic encephalopathy (HE) is a prevalent and debilitating condition characterized by cognitive disturbances in which ammonia and inflammation play a synergistic pathogenic role. Extraskeletal functions of vitamin D include immunomodulation, and its deficiency has been implicated in immune dysfunction and different forms of cognitive impairment. The aim was to assess changes in cognitive function and inflammation in decompensated patients with cirrhosis receiving vitamin D supplementation. &lt;b>Methods&lt;/b>: Patients with cirrhosis discharged from decompensation in two tertiary hospitals in Spain (from September 2017 to January 2020) were assessed before</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-04T22:25:00.496Z</modification><creation>2025-04-04T22:25:00.496Z</creation></dates><accession>S-EPMC11768058</accession><cross_references><pubmed>39861356</pubmed><doi>10.3390/nu17020226</doi></cross_references></HashMap>